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Get the free CHASING COVID Cohort specimen 4 collection demo video

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Version 2.1March 31, 2020We all have a role to play in slowing the spread of novel Coronavirus (aka SARS/COV2). Join the CHASE COVID-19 study to help contribute to our understanding of this pandemic,
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How to fill out chasing covid cohort specimen

01
Wear appropriate personal protective equipment (PPE) such as gloves, mask, and gown.
02
Identify the patient and confirm their information.
03
Explain the procedure to the patient and obtain their consent.
04
Collect a nasal or throat swab specimen from the patient.
05
Label the specimen container properly with the patient's information.
06
Place the specimen container in a biohazard bag for transportation.
07
Submit the specimen to the designated laboratory for testing.
08
Follow proper hand hygiene and dispose of PPE according to guidelines.
09
Document the procedure and specimen collection in the patient's medical record.

Who needs chasing covid cohort specimen?

01
Individuals who are part of a COVID-19 cohort study or research project.
02
Healthcare professionals conducting research on COVID-19.
03
Patients who are suspected or confirmed to have COVID-19 and need their specimens collected for testing or monitoring.
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Chasing COVID cohort specimen refers to the standardized process of collecting and analyzing specimens from a designated group of individuals for COVID-19 testing and research purposes.
Entities such as healthcare providers, laboratories, and research institutions that collect or analyze COVID-19 specimens are required to file the chasing COVID cohort specimen.
To fill out the chasing COVID cohort specimen, complete the designated form with accurate information regarding the specimen, including patient details, collection date, test performed, and results obtained.
The purpose of chasing COVID cohort specimen is to monitor and evaluate the spread of COVID-19, track variants, and conduct research related to the disease’s epidemiology and treatment.
Reported information must include patient demographics, specimen type, collection date, testing method, results, and any relevant clinical information.
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